FDA 510(k)

一次性血刺针

K号: K220387 · 2022-08-17

申请人Suzhou Kyuan Medical Apparatus Co., Ltd.

决定日期2022-08-17

产品代码QRL

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决定实质等同

器械摘要

Disposable Blood Lancets is the device name listed in this FDA 510(k) record. The listed applicant is Suzhou Kyuan Medical Apparatus Co., Ltd.. It received FDA 510(k) clearance on 2022-08-17 under 510(k) number K220387. The device is classified under product code QRL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Disposable Blood Lancets?

Disposable Blood Lancets is a medical device that received FDA 510(k) clearance on 2022-08-17. The listed applicant is Suzhou Kyuan Medical Apparatus Co., Ltd.. The 510(k) number is K220387.

When did Disposable Blood Lancets receive FDA 510(k) clearance?

Disposable Blood Lancets received FDA 510(k) clearance on 2022-08-17, under 510(k) number K220387.

Who is the listed applicant for Disposable Blood Lancets?

The FDA 510(k) record lists Suzhou Kyuan Medical Apparatus Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Disposable Blood Lancets?

The FDA product code for Disposable Blood Lancets is QRL.

列明Suzhou Kyuan Medical Apparatus Co., Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K221778一次性安全注射针

相关器械（代码：QRL）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K262135刺针Tianjin Huahong Technology Co., Ltd.K262211lancetTianjin Huahong Technology Co., Ltd.K260122穿刺器（PressGo, LDE3, LDE3AST, LDE5, EasyStep）SteriLance Medical (Suzhou), Inc.K253706刺针 (HH-XV-T)Tianjin Huahong Technology Co., Ltd.K250813MICROLET®NEXT 2 刺针装置Ascensia Diabetes Care U.S., Inc.K243306lancet (IA, IB, IC, ID, IE, IK, IL, IM, IIA, IIB, III, V, VI, VII, VIII, IX); 刺针 (HH-X-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T, HH-XXV-T, HH-XXVI-T, HH-XXVIII-T, HH-XXIX-T, HH-XXX-T, HH-XIII-T, HH-XXVII-T)Tianjin Huahong Technology Co., Ltd.

官方来源

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